Correction: Highly contiguous assemblies of 101 drosophilid genomes
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Kim BY, Wang JR, Miller DE, Barmina O, Delaney E, Thompson A, Comeault AA, Peede D, D'Agostino ERR, Pelaez J, Aguilar JM, Haji D, Matsunaga T, Armstrong EE, Zych M, Ogawa Y, Stamenković-Radak M, Jelić M, Veselinović MS, Tanasković M, Erić P, Gao J-J, Katoh TK, Toda MJ, Watabe H, Watada M, Davis JS, Moyle LC, Manoli G, Bertolini E, Košťál V, Hawley RS, Takahashi A, Jones CD, Price DK, Whiteman N, Kopp A, Matute DR, Petrov DA. 2021. Highly contiguous assemblies of 101 drosophilid genomes. eLife 10:e66405. doi: 10.7554/eLife.66405.
Published 19 July 2021
This review was prepared by Bernard Kim, Diler Haji, Noah Whiteman, Artyom Kopp, Daniel Matute, and Dmitri Petrov.
This correction is issued to correct the species identification of the Drosophila nebulosa 14030–0761.01 line from this study. Here, we show that strain 14030–0761.01 is not D. nebulosa, but instead D. sucinea, and that the line is likely misidentified at the stock center. It is unknown whether line 14030–0761.01 was originally D. nebulosa. Although we did not assemble the genome of D. sucinea 14030–0791.00, our analyses of genomic data from this strain also show that it is likely misidentified D. paulistorum.
Several genomes of drosophilid species belonging to the willistoni species group were assembled for this study. Among these were two closely related species purchased from the National Drosophila Species Stock Center (NDSSC) in December 2019: D. sucinea 14030–0791.01 and “D. nebulosa” 14030–0761.01. For clarity, we will refer to misidentified strains henceforth with the species name in quotes. After the publication of this manuscript, we were notified that our assembly of “D. nebulosa” 14030–0761.01 resembled D. sucinea more than other willistoni group species (pers. comm. Christopher Sottolano, Anthony Geneva, and Nir Yakoby). Indeed our “D. nebulosa” genome appears as a sister taxon to D. sucinea in our phylogeny, rather than the other willistoni group species we sequenced (Figure 5 of the original manuscript), inconsistent with other phylogenies inferred from molecular data (e.g., Finet et al., 2021).
We first wished to eliminate the possibility that we unknowingly sequenced D. sucinea multiple times due to sample mishandling. If so, the variation present in the long and short read datasets should not be consistent with two genetically distinct lines. To test for this, we built new genome assemblies to obtain a consensus sequence of the variation represented by each set of reads, then inferred the phylogenetic relationships of the new assemblies.
In addition to the willistoni group assemblies already generated through the hybrid approach in our previous work (including D. sucinea and “D. nebulosa”), we newly assembled our Nanopore and Illumina reads for D. sucinea 14030–0791.01 and “D. nebulosa” 14030–0761.01, and Illumina reads for “D. sucinea” 14030–0791.00 and D. nebulosa 14030–0761.00 (Khallaf et al., 2021; available from NCBI BioProject PRJNA669609). However, “D. sucinea” 14030–0791.00 was ignored for reasons we will cover shortly. We also obtained an unpublished draft assembly of D. nebulosa 14030–0761.06 courtesy of Christopher Sottolano and Nir Yakoby. Finally, our D. saltans assembly was used as an outgroup. Short read datasets were assembled with SPAdes v3.15.3 (Prjibelski et al., 2020). Nanopore reads were assembled with Flye 2.9 (Kolmogorov et al., 2019) then polished once with Oxford Nanopore’s Medaka software (v1.4.4). The 125 BUSCO genes (Manni et al., 2021) that were the most complete across all assemblies were used to build an ASTRAL tree (Zhang et al., 2018), using the methods from our study (Figure 1).
The phylogenetic relationships between the various samples showed us two important things (Figure 1). First, “D. nebulosa” 14030–0761.01 is indeed more closely related to D. sucinea than to the other D. nebulosa assemblies, confirming our suspicions that this line is misidentified. Second, the sequences from “D. nebulosa” 14030–0761.01 and D. sucinea 14030–0791.01 form clusters distinct from each other, meaning the samples were properly handled for sequencing.
While we originally downloaded “D. sucinea” 14030–0791.00 data from NCBI for these analyses, we found those data to be also inconsistent with the phylogeny and ignored them for this analysis. COI sequences extracted from these reads and queried at the Barcode of Life Database (Ratnasingham and Hebert, 2007) suggested these reads were instead from D. paulistorum. Mapping these sequences against our willistoni group assemblies was consistent with this species prediction: only 27.9% of reads mapped to our D. sucinea assembly while the best-mapping assembly was D. paulistorum 14030–0771.06, with 97.5% of reads mapped.
Although strain misidentification seems to explain the anomaly in our data, we sought to further clarify the species identity of the strain and the origin of the misidentification or contamination. To eliminate the possibility of contamination in strains maintained in our labs, we ordered nine fresh lines from the NDSSC: (four lines) D. nebulosa 14030–0761.00,01,03,06; (three lines) D. sucinea 14030–0791.00,01,02; D. capricorni 14030–0721.01; and D. willistoni 14030–0811.17. Sanger sequencing of the COI marker locus was performed for each strain and wings were examined for an anterior dark spot (Figure 2), a distinguishing characteristic of D. nebulosa (pers comm. A Kopp).
As expected, “D. nebulosa” 14030–0761.01 lacks the anterior pigmentation found in true D. nebulosa lines (Figure 2). A maximum likelihood phylogeny constructed with COI sequences (Figure 2) further supports our suspicions that the “D. nebulosa” misidentified line is D. sucinea and that “D. sucinea” 14030–0791.00 is not a D. sucinea line. The consistency between our data, data sequenced by others (Khallaf et al., 2021) and uploaded to NCBI, and the freshly obtained lines indicates “D. nebulosa” 14030–0761.01 and “D. sucinea” 14030–0791.00 strains are misidentified at the NDSSC. We have notified the NDSSC and recommend these strains be used with caution.
Other than revised table and figure text to correct the species misidentification, this issue does not affect any of the results presented by this work.
References to D. nebulosa are now revised to D. sucinea** in Figures 1, 2, 3, and 5. Figures legends and the underlying data have not changed.
The corrected Figure 1 is shown here:
For reference, the originally published Figure 1 is shown:
The corrected Figure 2 is shown here:
For reference, the originally published Figure 2 is shown:
The corrected Figure 3 is shown here:
For reference, the originally published Figure 3 is shown:
The corrected Figure 5 is shown here:
For reference, the originally published Figure 5 is shown:
Lastly, any references to D. nebulosa in Supplementary Files 1, 2, 3, 4, and 6, and Table 1, are now revised to D. sucinea**. No other entries in these tables are changed.
The article has been corrected accordingly.
Data accessibility: Wing photographs are available on Dryad (https://datadryad.org/stash/share/n7sjF2ckUQS2kTcEJJPPMyD4QOFoY0DbWQH9vRrXpfM). NCBI Accession numbers for new COI sequences are listed in Table 1.
References
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Assembly of long, error-prone reads using repeat graphsNature Biotechnology 37:540–546.https://doi.org/10.1038/s41587-019-0072-8
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Using SPAdes de novo assemblerCurrent Protocols in Bioinformatics 70:e102.https://doi.org/10.1002/cpbi.102
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BOLD: The Barcode of Life Data SystemMolecular Ecology Notes 7:355–364.https://doi.org/10.1111/j.1471-8286.2007.01678.x
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